famotidine

Generic: famotidine

Labeler: cardinal health 107, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name famotidine
Generic Name famotidine
Labeler cardinal health 107, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

famotidine 20 mg/1

Manufacturer
Cardinal Health 107, LLC

Identifiers & Regulatory

Product NDC 55154-4313
Product ID 55154-4313_934ab643-7f86-46f0-831a-f62f07db8989
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075718
Listing Expiration 2026-12-31
Marketing Start 2001-04-16

Pharmacologic Class

Established (EPC)
histamine-2 receptor antagonist [epc]
Mechanism of Action
histamine h2 receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 551544313
Hyphenated Format 55154-4313

Supplemental Identifiers

RxCUI
310273
UPC
0055154431309
UNII
5QZO15J2Z8
NUI
N0000000151 N0000175784

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name famotidine (source: ndc)
Generic Name famotidine (source: ndc)
Application Number ANDA075718 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 10 BLISTER PACK in 1 BAG (55154-4313-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (1)

55154-4313-0 10 BLISTER PACK in 1 BAG (55154-4313-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (1)

famotidine (20 mg/1)

Linked Drug Pages (1)

Famotidine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "934ab643-7f86-46f0-831a-f62f07db8989", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0055154431309"], "unii": ["5QZO15J2Z8"], "rxcui": ["310273"], "spl_set_id": ["5d515c2a-dac9-42d8-aede-66d28a427dbc"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-4313-0)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "55154-4313-0", "marketing_start_date": "20230315"}], "brand_name": "Famotidine", "product_id": "55154-4313_934ab643-7f86-46f0-831a-f62f07db8989", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "55154-4313", "generic_name": "Famotidine", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA075718", "marketing_category": "ANDA", "marketing_start_date": "20010416", "listing_expiration_date": "20261231"}